Canonical Allele Identifier: CA543045478
Gene: COL7A1 HGNC NCBI

Linked Data

dbSNP Id: rs1201807690
gnomAD v2: 3-48607683-C-T
gnomAD v3: 3-48570250-C-T
gnomAD v4: 3-48570250-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48570250C>T , CM000665.2:g.48570250C>T GRCh38
NC_000003.11:g.48607683C>T , CM000665.1:g.48607683C>T GRCh37
NC_000003.10:g.48582687C>T NCBI36
NG_007065.1:g.30003G>A , LRG_286:g.30003G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000681320.1:c.7440+25G>A MANE Select ENSP00000506558.1:n.7440+25G>A
ENST00000328333.12:c.7440+25G>A ENSP00000332371.8:n.7440+25G>A
ENST00000422991.1:c.435+25G>A ENSP00000391608.1:n.435+25G>A
ENST00000459756.5:n.192G>A
ENST00000467985.1:n.215G>A
ENST00000487017.5:n.4079+25G>A
NM_000094.3:c.7440+25G>A , LRG_286t1:c.7440+25G>A NP_000085.1:n.7440+25G>A
XM_011533336.1:c.7467+25G>A XP_011531638.1:n.7467+25G>A
XM_011533337.1:c.7440+25G>A XP_011531639.1:n.7440+25G>A
XM_011533338.1:c.7408-72G>A XP_011531640.1:n.7408-72G>A
XM_011533339.1:c.7467+25G>A XP_011531641.1:n.7467+25G>A
XM_011533340.1:c.7410G>A XP_011531642.1:p.Pro2470=
XM_011533341.1:c.7384G>A XP_011531643.1:p.Glu2462Lys
XM_011533342.1:c.7382-72G>A XP_011531644.1:n.7382-72G>A
XR_940369.1:n.7503+25G>A
XR_940370.1:n.7503+25G>A
XR_940371.1:n.7503+25G>A
XR_940372.1:n.7477+25G>A
XM_017005688.1:c.7381-72G>A XP_016861177.1:n.7381-72G>A
XM_017005689.1:c.7440+25G>A XP_016861178.1:n.7440+25G>A
XM_017005690.1:c.7383G>A XP_016861179.1:p.Pro2461=
XM_017005691.1:c.7357G>A XP_016861180.1:p.Glu2453Lys
XM_017005692.1:c.7355-72G>A XP_016861181.1:n.7355-72G>A
XR_001740003.1:n.7476+25G>A
XR_001740004.1:n.7476+25G>A
XR_001740005.1:n.7476+25G>A
XR_001740006.1:n.7450+25G>A
NM_000094.4:c.7440+25G>A MANE Select NP_000085.1:n.7440+25G>A